HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl 3-(4,4-difluoro-1-piperidyl)azetidine-1-carboxylate → 1-(Azetidin-3-YL)-4,4-difluoropiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl 3-(4,4-difluoro-1-piperidyl)azetidine-1-carboxylate | HCID 59606161 | — |
| Solvent | Trifluoroacetic acid methylene chloride | HCID 21863450 | — |
| Product | 1-(Azetidin-3-YL)-4,4-difluoropiperidine | HCID 59605315 | 64.1% |
Reaction Steps
A 25 mL round-bottomed flask was charged with a solution of 3-(4,4-difluoropiperidin-1-yl)azetidine-1-carboxylic acid tert-butyl ester (0.684 g, 2.47 mmol) in DCM/TFA (4 mL/4 mL). The reaction mixture was stirred for 3 h at room temperature. The reaction mixture was loaded onto an Isolute® SCX-2 cartridge. The cartridge was washed with MeOH and the desired product was eluted using 2 M NH3 in MeOH to give 1-Azetidin-3-yl-4,4-difluoropiperidine as a pale yellow oil (0.279 g, 64%). 1H NMR (CDCl3, 400 MHz) δ 3.64-3.54 (m, 4H); 3.30-3.25 (m, 1H); 2.43-2.37 (m, 4H); 2.06-1.93 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08173650B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-0cf5066743a246ab98e5659177ff66b6 |
| Source note | uspto-grants-2012_05 |